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67527-71-3

67527-71-3 Structure

67527-71-3 Structure
IdentificationBack Directory
[Name]

Mildiomycin
[CAS]

67527-71-3
[Synonyms]

TF-138
midomycin
Mildiomycin
Antibiotic B-98891
4-Amino-1-[4-[[(S)-2-amino-3-hydroxy-1-oxopropyl]amino]-9-guanidino-6-carboxy-2,3,4,7,9-pentadeoxy-α-L-talo-non-2-enopyranosyl]-5-(hydroxymethyl)pyrimidin-2(1H)-one
4-Amino-1-[4-[[(S)-2-amino-3-hydroxy-1-oxopropyl]amino]-9-guanidino-6-carboxy-2,3,4,7,9-pentadeoxy-α-L-talo-nona-2-enopyranosyl]-5-(hydroxymethyl)pyrimidin-2(1H)-one
2(1H)-Pyrimidinone, 4-amino-1-[4-[[(2S)-2-amino-3-hydroxy-1-oxopropyl]amino]-9-[(aminoiminomethyl)amino]-6-C-carboxy-2,3,4,7,9-pentadeoxy-α-L-talo-non-2-enopyranosyl]-5-(hydroxymethyl)-
[Molecular Formula]

C19H30N8O9
[MDL Number]

MFCD01939748
[MOL File]

67527-71-3.mol
[Molecular Weight]

514.49
Chemical PropertiesBack Directory
[Melting point ]

>300° (monohydrate)
[alpha ]

D20 +100° (c = 0.5 in water); +78.5° (c = 0.5 in 0.1N HCl)
[density ]

1.81±0.1 g/cm3(Predicted)
[pka]

2.8, 4.3, 7.2, >12(at 25℃)
Hazard InformationBack Directory
[Description]

Mildiomycin is a nucleoside antibiotic isolated from the culture filtrate of Streptoverticillium rimofaciens B-98891 (17). C19H30N8O9 (514.5). Basic and hygroscopic. Solubility: In water 580 g/L; in methanol 480; ethanol 160 (mg/L). Insoluble in ethyl acetate and ethyl ether. Susceptible to photodegradation by sunlight.
[Uses]

Specifically active against the powdery mildew pathogens; excellent curative activity on the disease of various plants in vivo.Used in practice for the control of powderymildews on rose, spindle tree, and Indian lilac.
[Toxicity evaluation]

Mildiomycin remarkably inhibits protein synthesis in E. coli. The synthesis of polypeptides in mammalian cellfree system from rabbit reticulocytes is less sensitive to mildiomycin than that from E. coli (18). The toxicity of mildiomycin is low; LD50 for acute toxicity in rats and mice is 500–1000 mg/kg by intravenous and subcutaneous injections, and 2.5–5.0 g/kg by oral administration. At a concentration of 1000 ppm, there is no irritation to the cornea and skin of rabbits for 10 days.
Safety DataBack Directory
[Toxicity]

LD50 in rats, mice: ~500-1000 mg/kg i.v.; ~2.5-5.0 g/kg orally (Harada, Kishi)
67527-71-3 suppliers list
Company Name: Shaanxi Cuikang Pharmaceutical Technology Co., Ltd
Tel: +86-18791163155 +86-13119157289 , +86-13119157289
Website: www.cuikangmed.com/
Company Name: CHEMICAL LAND21  
Tel: 82- 2 -783 - 8063
Website: www.chemicalland21.com
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